Aerosol and rain samples were collected between 48°N and 55°S during the KH-08-2 and MR08-06 cruises conducted over the North and South Pacific Ocean in 2008 and, to estimate dry and wet deposition fluxes of atmospheric inorganic nitrogen (N). Inorganic N in aerosols was composed of~68% NH 4 + and~32% NO 3 -(median values for all data), with~81% and~45% of each species being present on fine mode aerosol, respectively. Concentrations of NH 4 + and NO 3 − in rainwater ranged from 1.7-55 μmol L −1 and 0.16-18 μmol L −1 , respectively, accounting for~87% by NH 4 + and~13% by NO 3 − of total inorganic N (median values for all data). A significant correlation (r00.74, p<0.05, n010) between NH 4 + and methanesulfonic acid (MSA) was found in rainwater samples collected over the South Pacific, whereas no significant correlations were found between NH 4 + and MSA in rainwater collected over the subarctic (r0 0.42, p>0.1, n06) and subtropical (r00.33, p>0.5, n06) western North Pacific, suggesting that emissions of ammonia (NH 3 ) by marine biological activity from the ocean could become a significant source of NH 4 + over the South Pacific. While NO 3 − was the dominant inorganic N species in dry deposition, inorganic N supplied to surface waters by wet deposition was predominantly by NH 4 + (42-99% of the wet deposition fluxes for total inorganic N). We estimated mean total (dry+wet) deposition fluxes of atmospheric total inorganic N in the Pacific Ocean to be 32-64 μmol m −2 d −1 , with 66-99% of this by wet deposition, indicating that wet deposition plays a more important role in the supply of atmospheric inorganic N than dry deposition.